Suz and Katrina | Picture Day

Raise your hand if you have memories of elementary school picture day…Did they pass out those little plastic combs? Anybody have some really terrible pictures to share? Today, Katrina and Suz talk about what happens when picture day is really more than just picture day.  When your child is facing rare disease, with a shortened life expectancy, you never know when this picture day is the last picture day they will have. The girls talk about making the memories, soaking in the moments, and normalizing grief. “You never know what’s going to be the last picture because you can’t trust the disease.” -Suz Here’s what you don’t want to miss: Picture Day What if? The last picture When it doesn’t make sense Take the pictures Normalizing Grief Have you ever found yourself doing something that seems just so crazy, in the name of grief? Let us know in the When Autumn Comes Society or send us a DM on Instagram! We’d love to hear from you! While you’re at it, consider supporting the podcast . When Autumn Comes: WAC Instagram WAC Facebook Page WAC Society Facebook Page WAC is a program of the Apricity Hope Project Apply for a Caregiver Package

Om Podcasten

We call ourselves the 4am Mom Club because more nights than not, our kids are awake at 4am. We both have very medical, complicated, rare, beautiful children. This is a podcast for medical and disability mamas (and the people who love them) who are facing a life they never expected. We share hope-filled stories of families, all shapes, colors, sizes and abilities, all in different phases of their medically complex or disabled caregiving journey. When Autumn Comes Podcast is a program of the Apricity Hope Project nonprofit. Our mission is to care for caregiver. Learn more at apricityhope.org